| Literature DB >> 27497620 |
Manuel V Borca1, Vivian O'Donnell2, Lauren G Holinka1, Devendra K Rai2, Brenton Sanford3, Marialexia Alfano4, Jolene Carlson5, Paul A Azzinaro4, Covadonga Alonso6, Douglas P Gladue7.
Abstract
African swine fever virus (ASFV) is the etiological agent of a contagious and often lethal disease of domestic pigs that has significant economic consequences for the swine industry. The viral genome encodes for more than 150 genes, and only a select few of these genes have been studied in some detail. Here we report the characterization of open reading frame Ep152R that has a predicted complement control module/SCR domain. This domain is found in Vaccinia virus proteins that are involved in blocking the immune response during viral infection. A recombinant ASFV harboring a HA tagged version of the Ep152R protein was developed (ASFV-G-Ep152R-HA) and used to demonstrate that Ep152R is an early virus protein. Attempts to construct recombinant viruses having a deleted Ep152R gene were consistently unsuccessful indicating that Ep152R is an essential gene. Interestingly, analysis of host-protein interactions for Ep152R using a yeast two-hybrid screen, identified BAG6, a protein previously identified as being required for ASFV replication. Furthermore, fluorescent microscopy analysis confirms that Ep152R-BAG6 interaction actually occurs in cells infected with ASFV. Published by Elsevier B.V.Entities:
Keywords: ASF; ASFV; African swine fever virus; BAG6; Viral-host interactions
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Year: 2016 PMID: 27497620 DOI: 10.1016/j.virusres.2016.07.013
Source DB: PubMed Journal: Virus Res ISSN: 0168-1702 Impact factor: 3.303